Stich Maximilian, Benning Louise, Speer Claudius, Garbade Sven F, Bartenschlager Marie, Kim Heeyoung, Jeltsch Kathrin, Tabatabai Julia, Niesert Moritz, Janda Aleš, Renk Hanna, Elling Roland, Hoffmann Georg Friedrich, Kräusslich Hans-Georg, Müller Barbara, Bartenschlager Ralf, Tönshoff Burkhard
Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
J Med Virol. 2023 Mar;95(3):e28582. doi: 10.1002/jmv.28582.
Data on cross-neutralization of the SARS-CoV-2 omicron variant more than 1 year after SARS-CoV-2 infection are urgently needed, especially in children, to predict the likelihood of reinfection and to guide vaccination strategies. In a prospective observational cohort study, we evaluated live-virus neutralization of the SARS-CoV-2 omicron (BA.1) variant in children compared with adults 14 months after mild or asymptomatic wild-type SARS-CoV-2 infection. We also evaluated immunity to reinfection conferred by previous infection plus COVID-19 mRNA vaccination. We studied 36 adults and 34 children 14 months after acute SARS-CoV-2 infection. While 94% of unvaccinated adults (16/17) and children (32/34) neutralized the delta (B.1.617.2) variant, only 1/17 (5.9%) unvaccinated adults, 0/16 (0%) adolescents and 5/18 (27.8%) children <12 years of age had neutralizing activity against omicron (BA.1). In convalescent adults, one or two doses of mRNA vaccine increased delta and omicron neutralization 32-fold, similar to a third mRNA vaccination in uninfected adults. Neutralization of omicron was 8-fold lower than that of delta in both groups. In conclusion, our data indicate that humoral immunity induced by previous SARS-CoV-2 wild-type infection more than 1 year ago is insufficient to neutralize the current immune escape omicron variant.
迫切需要感染新冠病毒超过1年的人群中关于新冠病毒奥密克戎变异株交叉中和的数据,尤其是儿童的数据,以预测再次感染的可能性并指导疫苗接种策略。在一项前瞻性观察队列研究中,我们评估了在轻度或无症状野生型新冠病毒感染14个月后,儿童与成人对新冠病毒奥密克戎(BA.1)变异株的活病毒中和情况。我们还评估了既往感染加新冠病毒mRNA疫苗接种所赋予的对再次感染的免疫力。我们研究了急性新冠病毒感染14个月后的36名成人和34名儿童。虽然94%未接种疫苗的成人(16/17)和儿童(32/34)能够中和德尔塔(B.1.617.2)变异株,但只有1/17(5.9%)未接种疫苗的成人、0/16(0%)青少年和5/18(27.8%)12岁以下儿童对奥密克戎(BA.1)有中和活性。在康复成人中,一剂或两剂mRNA疫苗使德尔塔和奥密克戎的中和能力提高了32倍,这与未感染成人接种第三剂mRNA疫苗的效果相似。两组中奥密克戎的中和能力均比德尔塔低8倍。总之,我们的数据表明,1年多前既往新冠病毒野生型感染所诱导的体液免疫不足以中和当前具有免疫逃逸能力的奥密克戎变异株。